Format

Send to

Choose Destination
Am J Blood Res. 2013 Aug 19;3(3):225-38. eCollection 2013.

Treatment of severe steroid resistant acute GVHD with mesenchymal stromal cells (MSC).

Author information

1
Department of Bone Marrow Transplantation and Cancer Immunotherapy, Hadassah-Hebrew University Medical Center Jerusalem.

Abstract

BACKGROUND:

Several studies revealed that MSC from human bone marrow can downregulate graft-versus-host disease (GVHD) after allogeneic HSCT.

METHODS:

Herein we present 50 patients with acute GVHD who got 74 (1-4) MSC infusions for 54 separate episodes of aGVHD.

RESULTS:

aGVHD was defined as steroid resistant grade IV aGVHD in 42 cases. The major presentation was gastrointestinal GVHD; two (n=18) or more (n=21) systems were involved in the majority of cases. The 1(st) infusion with MSC was given on day +27 (range, 1 to 136); d+45 (range, +11 to +150) post diagnosis of aGVHD and HSCT, respectively. In 2/3 of the cases treatment was performed with frozen stocked MSCs; in 62 cases early passages (1-3) were used. The median number of infused cells was 1.14±0.47 million per kg in the first injection and up to 4.27 (1.70±1.10) millions in total. The two patients with aggressive liver GVHD received MSCs injections intra hepatic arteries without changes of blood flow or evidence cytolysis, but also without a visible effect. Disease free survival at 3.6 years was 56%. We observed better overall survival in patients with GVHD grade < 4, in responders to the 1(st) treatment with MSC, and in pediatric group. The multivariate analysis demonstrated independent influence on survival of initial response and younger age. There were no immediate or late toxicity or side effects.

CONCLUSION:

Injection of MSCs seems to be a promising and safe treatment of GVHD. The encouraging results obviously should be confirmed in a randomized prospective study.

KEYWORDS:

Mesenchymal stromal cells (MSC); graft versus host disease; hematopoietic stem cell transplantation; mesenchymal stem cells; steroid resistance

PMID:
23997985
PMCID:
PMC3755522

Supplemental Content

Full text links

Icon for PubMed Central
Loading ...
Support Center